期刊文献+

Glucose production from hydrolysis of cellulose over a novel silica catalyst under hydrothermal conditions 被引量:1

Glucose production from hydrolysis of cellulose over a novel silica catalyst under hydrothermal conditions
原文传递
导出
摘要 A novel silica catalyst was synthesized by evaporation-induced self-assembly (EISA) method and tested for the catalytic selective hydrolysis of cellulose to glucose. This silica catalyst exhibited a higher catalytic activity than other oxides prepared by the same method, such as ZrO2, TiO2, and Al2O3. Using silica as a catalyst, cellulose was selectively hydrolyzed into glucose with a glucose yield as high as 50% under hydrothermal conditions without hydrogen gas. The silica catalyst was characterized by Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD) and transmission electron microscopy (TEM). The results of temperature-programmed desorption of ammonia (NH3-TPD) and textural properties indicated that the synergistic effect between strong acidity and a suitable pore diameter of the silica catalyst may be responsible for its high activity. In addition, the catalyst was recyclable and showed excellent stability during the recycle catalytic runs. A novel silica catalyst was synthesized by evaporation-induced self-assembly (EISA) method and tested for the catalytic selective hydrolysis of cellulose to glucose. This silica catalyst exhibited a higher catalytic activity than other oxides prepared by the same method, such as ZrO2, TiO2, and Al2O3. Using silica as a catalyst, cellulose was selectively hydrolyzed into glucose with a glucose yield as high as 50% under hydrothermal conditions without hydrogen gas. The silica catalyst was characterized by Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD) and transmission electron microscopy (TEM). The results of temperature-programmed desorption of ammonia (NH3-TPD) and textural properties indicated that the synergistic effect between strong acidity and a suitable pore diameter of the silica catalyst may be responsible for its high activity. In addition, the catalyst was recyclable and showed excellent stability during the recycle catalytic runs.
出处 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2012年第3期473-478,共6页 环境科学学报(英文版)
基金 supported by the National Natural Science Found for Creative Research Groups of China (No.50921604)
关键词 CELLULOSE GLUCOSE silica catalyst HYDROLYSIS HYDROTHERMAL biomass cellulose glucose silica catalyst hydrolysis hydrothermal biomass
  • 相关文献

参考文献25

  • 1Abbadi A,Gotlieb K F,van Bekkum H,1998.Study on solidacid catalyzed hydrolysis of maltose and related polysac-charides.Starch,50(1): 23–28.
  • 2Deguchi S,Tsujiib K,Horikoshi K,2008.Crystalline-to-amorphous transformation of cellulose in hot and compressed water and its implications for hydrothermal conver-sion.Green Chemistry,10(2): 191–196.
  • 3Deng W P,Tan X S,Fang W H,Zhang Q H,Wang Y,2009.Conversion of cellulose into sorbitol over carbon nanotube-supported ruthenium catalyst.Catalysis Letters,133(1-2):167–174.
  • 4Dhepe P L,Ohashi M,Inagaki S,Ichikawa M,Fukuoka A,2005.Hydrolysis of sugars catalyzed by watertolerant sulfonatedmesoporous silicas.Catalysis Letters,102(3-4): 163–169.
  • 5Farrell A E,Plevin R J,Turner B T,Jones A D,O’Hare M,Kammen D M,2006.Ethanol can contribute to energy andenvironmental goals.Science,311(5760): 506–508.
  • 6Fukuoka A,Dhepe P L,2006.Catalytic conversion of celluloseinto sugar alcohols.Angewandte Chemie International Edi-tion,45(31): 5161–5163.
  • 7Ji N,Zhang T,Zheng M Y,Wang A Q,Wang H,Wang X D et al.,2008.Direct catalytic conversion of cellulose into ethyleneglycol using nickel-promoted tungsten carbide catalysts.Angewandte Chemie International Edition,47(44): 8510–8513.
  • 8Klemm D,Heublein B,Fink H P,Bohn A,2005.Cellulose:fascinating biopolymer and sustainable raw material.Ange-wandte Chemie International Edition,44(22): 3358–3393.
  • 9Langan P,Nishiyama Y,Chanzy H,2001.X-ray structure of mer-cerized Cellulose II at 1 resolution.Biomacromolecules,2(2): 410–416.
  • 10Luo C,Wang S,Liu H C,2007.Cellulose conversion into polyolscatalyzed by reversibly formed acids and supported rutheni-um clusters in hot water.Angewandte Chemie InternationalEdition,46(40): 7636–7639.

引证文献1

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部